TY - JOUR
T1 - A multicenter REtrospective observational study of first-line treatment with PERtuzumab, trastuzumab and taxanes for advanced HER2 positive breast cancer patients. RePer Study
AU - Gamucci, Teresa
AU - Pizzuti, Laura
AU - Natoli, Clara
AU - Mentuccia, Lucia
AU - Sperduti, Isabella
AU - Barba, Maddalena
AU - Sergi, Domenico
AU - Iezzi, Laura
AU - Maugeri-Saccà, Marcello
AU - Vaccaro, Angela
AU - Magnolfi, Emanuela
AU - Gelibter, Alain
AU - Barchiesi, Giacomo
AU - Magri, Valentina
AU - D’Onofrio, Loretta
AU - Cassano, Alessandra
AU - Rossi, Ernesto
AU - Botticelli, Andrea
AU - Moscetti, Luca
AU - Omarini, Claudia
AU - Fabbri, Maria Agnese
AU - Scinto, Angelo Fedele
AU - Corsi, Domenico
AU - Corsi, Domenico Cristiano
AU - Carbognin, Luisa
AU - Mazzotta, Marco
AU - Bria, Emilio
AU - Foglietta, Jennifer
AU - Samaritani, Riccardo
AU - Garufi, Carlo
AU - Mariani, Luciano
AU - Barni, Sandro
AU - Mirabelli, Rosanna
AU - Sarmiento, Roberta
AU - Graziano, Vincenzo
AU - Santini, Daniele
AU - Marchetti, Paolo
AU - Tonini, Giuseppe
AU - Di Lauro, Luigi
AU - Sanguineti, Giuseppe
AU - Paoletti, Giancarlo
AU - Tomao, Silverio
AU - De Maria Marchiano, Ruggero
AU - Veltri, Enzo
AU - Paris, Ida
AU - Giotta, Francesco
AU - Latorre, Agnese
AU - Giordano, Antonio
AU - Ciliberto, Gennaro
AU - Vici, Patrizia
PY - 2019
Y1 - 2019
N2 - We carried out a retrospective observational study of 264 HER2-positive advanced breast cancer (ABC) patients to explore the efficacy of first-line treatment with pertuzumab/trastuzumab/taxane in real-world setting. Survival data were analyzed by Kaplan Meier curves and log rank test. Median follow-up, length of pertuzumab/trastuzumab/taxane treatment and of pertuzumab, trastuzumab maintenance were 21, 4 and 15 months, respectively. The response rate was 77.3%, and the clinical benefit rate 93.6%. Median progression-free survival (mPFS) was 21 months, and median overall survival (mOS) was not reached. When comparing patients by trastuzumab-pretreatment, similar PFS were observed, although a longer OS was reached in trastuzumab-naïve patients (p = 0.02). Brain metastases at baseline and their development in course of therapy were associated with significantly shorter PFS (p = 0.0006) and shorter OS, although at a not fully statistically relevant extent (p = 0.06). The addition of maintenance endocrine therapy (ET) to pertuzumab/trastuzumab maintenance was associated with longer PFS (p = 0.0001), although no significant differences were detected in OS (p = 0.31). Results were confirmed by propensity score analysis (p = 0.003 and p = 0.46, respectively). In multivariate models, longer PFS was related to lower Performance Status (PS) (p = 0.07), metastatic stage at diagnosis (p = 0.006) and single metastatic site (p < 0.0001). An OS advantage was observed with lower PS (p < 0.0001), single metastatic site (p = 0.004), no prior exposure to trastuzumab (p = 0.004) and response to pertuzumab-based treatment (p = 0.003). Our results confirm that trastuzumab/pertuzumab/taxane is the standard of care as first-line treatment of patients with HER2-positive ABC even in the real-world setting. Moreover, the double-maintenance therapy (HER2 block and ET) is strongly recommended when feasible.
AB - We carried out a retrospective observational study of 264 HER2-positive advanced breast cancer (ABC) patients to explore the efficacy of first-line treatment with pertuzumab/trastuzumab/taxane in real-world setting. Survival data were analyzed by Kaplan Meier curves and log rank test. Median follow-up, length of pertuzumab/trastuzumab/taxane treatment and of pertuzumab, trastuzumab maintenance were 21, 4 and 15 months, respectively. The response rate was 77.3%, and the clinical benefit rate 93.6%. Median progression-free survival (mPFS) was 21 months, and median overall survival (mOS) was not reached. When comparing patients by trastuzumab-pretreatment, similar PFS were observed, although a longer OS was reached in trastuzumab-naïve patients (p = 0.02). Brain metastases at baseline and their development in course of therapy were associated with significantly shorter PFS (p = 0.0006) and shorter OS, although at a not fully statistically relevant extent (p = 0.06). The addition of maintenance endocrine therapy (ET) to pertuzumab/trastuzumab maintenance was associated with longer PFS (p = 0.0001), although no significant differences were detected in OS (p = 0.31). Results were confirmed by propensity score analysis (p = 0.003 and p = 0.46, respectively). In multivariate models, longer PFS was related to lower Performance Status (PS) (p = 0.07), metastatic stage at diagnosis (p = 0.006) and single metastatic site (p < 0.0001). An OS advantage was observed with lower PS (p < 0.0001), single metastatic site (p = 0.004), no prior exposure to trastuzumab (p = 0.004) and response to pertuzumab-based treatment (p = 0.003). Our results confirm that trastuzumab/pertuzumab/taxane is the standard of care as first-line treatment of patients with HER2-positive ABC even in the real-world setting. Moreover, the double-maintenance therapy (HER2 block and ET) is strongly recommended when feasible.
KW - Cancer Research
KW - HER2
KW - Molecular Medicine
KW - Oncology
KW - Pharmacology
KW - endocrine therapy
KW - first-line treatment
KW - maintenance
KW - metastatic breast cancer
KW - pertuzumab
KW - trastuzumab
KW - Cancer Research
KW - HER2
KW - Molecular Medicine
KW - Oncology
KW - Pharmacology
KW - endocrine therapy
KW - first-line treatment
KW - maintenance
KW - metastatic breast cancer
KW - pertuzumab
KW - trastuzumab
UR - http://hdl.handle.net/10807/128350
UR - http://www.tandfonline.com/loi/kcbt20
U2 - 10.1080/15384047.2018.1523095
DO - 10.1080/15384047.2018.1523095
M3 - Article
SN - 1538-4047
VL - 20
SP - 192
EP - 200
JO - CANCER BIOLOGY & THERAPY
JF - CANCER BIOLOGY & THERAPY
ER -